• Genmab (Plainsboro, NJ)
    …and authentic is essential to fulfilling our purpose.The RoleThe Global Regulatory Labeling Strategy Sr Manager/Associate Director will be responsible for ... be within Global Regulatory Affairs (GRA) and will report to the Sr Director , Labeling , Policy and Intelligence. The position will be based in our Princeton, New… more
    HireLifeScience (11/15/24)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …and immune disorders. Summary This position serves as the Global Regulatory Affairs (GRA) Labeling Strategy expert to the Global Product Team (GPT) as an ad hoc ... member and independently provides strategic and operational leadership on new product labeling in collaboration with the Global Regulatory Leads (GRLs) and Clinical… more
    HireLifeScience (11/20/24)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …and immune disorders. SummaryThis position serves as the Global Regulatory Affairs (GRA) Labeling Strategy expert to the Global Product Team (GPT) as an ad hoc ... member and independently provides strategic and operational leadership on new product labeling in collaboration with the Global Regulatory Leads (GRLs) and Clinical… more
    HireLifeScience (11/02/24)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …rare diseases and immune disorders. Summary This position serves as the GRA labeling expert to the Global Regulatory Team (GRT) and independently provides strategic ... and operational leadership on product labeling in collaboration with Global Regulatory Leads (GRLs). This...hoc member of Global Project Team (GPT) to address labeling issues for late stage projects. This position manages… more
    HireLifeScience (01/06/25)
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  • Merck & Co. (Rahway, NJ)
    …clinical trials.- Global Clinical Supply is accountable for the planning, sourcing, labeling , packaging and delivery of clinical supplies to clinical sites globally. ... Development Teams.- Responsible for authoring clinical supply documentation in support of labeling and packaging activities as well as supply chain documentation to… more
    HireLifeScience (01/16/25)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …for license renewals, responses to Health Authority)Participant and voting member in the labeling development process in the Labeling Working Team (LWT), in ... collaboration with the CDLContributes from a medical strategy standpoint to developing the Clinical Study Report (CSR). May review tables, listings, and figures (TLF) and CSR safety narrativesMay lead the development and updates of the Investigator's Brochure… more
    HireLifeScience (01/17/25)
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  • Genmab (Plainsboro, NJ)
    …will join a highly competent global team focused on packaging and labeling clinical trial supplies, collaborating closely with the Global Clinical Drug Supply ... a can-do attitude to achieve results.You will be reporting to Director , Global Clinical Drug Supply in Copenhagen, Denmark.Main Responsibilities IncludeEngage with… more
    HireLifeScience (12/19/24)
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  • Director Labeling

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …and immune disorders. **Summary** This position serves as the Global Regulatory Affairs (GRA) Labeling Strategy expert to the Global Product Team (GPT) as an ad hoc ... member and independently provides strategic and operational leadership on new product labeling in collaboration with the Global Regulatory Leads (GRLs) and Clinical… more
    Daiichi Sankyo Inc. (11/20/24)
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  • Associate Director , Global Regulatory…

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …rare diseases and immune disorders. Summary This position serves as the GRA labeling expert to the Global Regulatory Team (GRT) and independently provides strategic ... and operational leadership on product labeling in collaboration with Global Regulatory Leads (GRLs). This...hoc member of Global Project Team (GPT) to address labeling issues for late stage projects. This position manages… more
    Daiichi Sankyo Inc. (01/18/25)
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  • Director , Global Regulatory Leader (GRL)

    J&J Family of Companies (Raritan, NJ)
    Johnson & Johnson Innovative Medicine is recruiting for a Director , Global Regulatory Leader. This position can be located in Spring House, PA; Horsham, PA; ... potential. At Johnson & Johnson, we all belong. The Director , Global Regulatory Leader, is responsible for global regulatory...Regulatory Team (GRT): + Serve as a member of Labeling Working Group (LWG) to build or update the… more
    J&J Family of Companies (12/10/24)
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  • Quality Assurance Director

    Compass Group, North America (New York, NY)
    …but the start of a career where you can flourish. Job Summary The Director of Quality Assurance will lead the development and execution of comprehensive QA programs ... requirements. + Oversee the Allergen Preventive Controls Program, ensuring accurate allergen labeling and prevention of cross-contact in line with Kirkland & Ellis… more
    Compass Group, North America (01/03/25)
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  • Senior Director , Oncology R&D

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …centered around rare diseases and immune disorders. **Summary** The Senior Director sits within Global Oncology Clinical Development, an organization dedicated to ... to Health Authority) + Participant and voting member in the labeling development process in the Labeling Working Team (LWT), in collaboration with the CDL +… more
    Daiichi Sankyo Inc. (01/01/25)
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  • Director , Sustainable Policy Compliance…

    L'Oreal USA (Clark, NJ)
    …/ Job Search (https://careers.loreal.com/en\_US/jobs/SearchJobs) / 196762 Director , Sustainable Policy Compliance Implementation Clark, NJ, ... NJ Corporate Responsibility Full - Time 17-Jan-2025 Job Title: Director , Sustainable Policy Compliance Implementation Division: Corporate Department: Sustainability… more
    L'Oreal USA (01/18/25)
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  • Director , Regulatory Affairs-Late Stage…

    Mitsubishi Chemical Group (Jersey City, NJ)
    …real-world evidence, and creating hope for all facing illness. The Director , Regulatory Affairs provides strategic global regulatory guidance to cross-functional ... and/or in the rare disease space. In this role, the Director defines and implements regulatory strategies; works with cross-functional project teams… more
    Mitsubishi Chemical Group (01/16/25)
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  • Sr. Director , Global Heath Literacy…

    Merck (Rahway, NJ)
    …their results, document disclosure, and data sharing with external researchers. The Senior Director of Global Health Literacy & Health Equity is the enterprise lead ... & Health Literacy Investigator Studies Program + Drive innovative patient labeling initiative to enhance product communication post-approval. + Incorporate health… more
    Merck (01/03/25)
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  • Sterile Processing Assistant Director

    Compass Group, North America (New York, NY)
    …Ambulatory EVS. Learn more at www.Crothall.com. Job Summary Working as an Assistant Director , you will be responsible for directing and leading all aspects of the ... the cleanliness of work areas + Supervises the requisitioning, sorting, labeling , and issuance of professional equipment + Coordinates sterilization, assembly, and… more
    Compass Group, North America (01/13/25)
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  • Associate Director , Clinical Supply…

    Merck (Rahway, NJ)
    …clinical trials. Global Clinical Supply is accountable for the planning, sourcing, labeling , packaging and delivery of clinical supplies to clinical sites globally. ... Teams. + Responsible for authoring clinical supply documentation in support of labeling and packaging activities as well as supply chain documentation to support… more
    Merck (01/16/25)
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  • Associate Director , Regulatory Affairs…

    Gilead Sciences, Inc. (Parsippany, NJ)
    …strategic and operational regulatory guidance on new concepts, campaigns, and product labeling for the assigned brands. You may manage complex interactions related ... RA Ad/Promo at Regulatory Project Team meetings. + Represents RA Ad/Promo at labeling meetings and provides strategic regulatory guidance. + Mentors RA Ad/Promo and… more
    Gilead Sciences, Inc. (11/16/24)
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  • Associate Director , Regulatory Affairs (In…

    Bristol Myers Squibb (Madison, NJ)
    …with HA deadlines. + Contribute in the developing of target labeling . **Degree / Experience Requirements** + Bachelor's degree required; advanced scientific ... degree preferred (Masters, PhD, PharmD, BSN, etc.) with 5 years in the industry with at least 4+ years of US Medical Device Regulatory Affairs experience **Key Competencies** + Experience in successfully leading teams; ability to broadly represent the… more
    Bristol Myers Squibb (01/03/25)
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  • Compliance Specialist

    Carter's/OshKosh (New York, NY)
    …at Carter's. **HOW YOU'LL MAKE AN IMPACT:** This role typically reports into the Sr Director , Quality Assurance and is based in our Skip Hop New York office. The ... into the office 3 days a week. 40%: Regulatory Labeling , Warnings, and Restrictions + Act as subject matter...Act as subject matter expert for product and packaging labeling requirements for all Skip Hop categories and countries.… more
    Carter's/OshKosh (01/17/25)
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